Allele Registry

Canonical Allele Identifier: PA2573074231

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Gly695Val	CA225451 NM_001377265.1:c.2084G>T